sodium O,O-diisopropyl dithiophosphate

Base Information

Chemical Name:sodium O,O-diisopropyl dithiophosphate
CAS No.:27205-99-8
Molecular Formula:C6H15 O2 P S2 . Na
Molecular Weight:236.271
Hs Code.:2931900090
Mol file:27205-99-8.mol

Synonyms:Isopropylsodium phosphorodithioate ((C3H7O)2(NaS)PS) (7CI); Phosphorodithioic acid,O,O-bis(1-methylethyl) ester, sodium salt (9CI); Phosphorodithioic acid,O,O-diisopropyl ester, sodium salt (8CI); Hostaflot LIP; Nadis; SodiumO,O-diisopropyl dithiophosphate; Sodium O,O-diisopropyl phosphorodithioate;Sodium O,O'-diisopropyldithiophosphate; Sodium diisopropyl phosphorodithioate;Sodium diisopropyldithiophosphate

Suppliers and Price of sodium O,O-diisopropyl dithiophosphate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 11 raw suppliers

Chemical Property of sodium O,O-diisopropyl dithiophosphate

Chemical Property:

Melting Point:189 °C
Boiling Point:257.1°Cat760mmHg
PKA:7.69[at 20 ℃]
Flash Point:109.3°C
PSA：60.36000
Density:1.145g/cm³
LogP:3.25840
Water Solubility.:1000g/L at 20℃

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Sodium O,O-Diisopropyl Dithiophosphate is an intermediate for the synthesis of Bensulide (B166000), which is an organophosphate acetylcholinesterase inhibitor used as an herbicide (1) in the protection of crops through pesticides (2). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.

Technology Process of sodium O,O-diisopropyl dithiophosphate

There total 3 articles about sodium O,O-diisopropyl dithiophosphate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 3031-21-8
bis(O,O-diisopropoxyphosphinothioyl)disulfide

: 123381-62-4
N-methyl-4-chlorobenzohydroxamic acid sodium salt

: 1144028-83-0
N-methyl-N-diisopropoxyphosphinothioyloxy-4-chlorobenzamide

: 27205-99-8
sodium O,O-diisopropyl dithiophosphate

Guidance literature:: N-methyl-4-chlorobenzohydroxamic acid sodium salt; With sodium hydride; In tetrahydrofuran; for 1.5h; Heating;

bis(O,O-diisopropoxyphosphinothioyl)disulfide; In tetrahydrofuran; at 20 ℃; for 0.333333h; Further stages.;
DOI:10.1002/hc.20423

Reference yield: 91.0%

: 84913-97-3,86118-20-9,1078716-00-3
antimony tris(O,O-diisopropyl phosphorodithioate)

: 27205-99-8
sodium O,O-diisopropyl dithiophosphate

Guidance literature:: With sodium pyrrolide; In tetrahydrofuran; for 2h; Ambient temperature;

Reference yield:

: 67-63-0,8013-70-5
isopropyl alcohol

: 27205-99-8
sodium O,O-diisopropyl dithiophosphate

Guidance literature:: isopropyl alcohol; With tetraphosphorus decasulfide; In benzene; at 60 ℃; for 1h;

With sodium hydroxide;
DOI:10.1016/S1386-1425(01)00707-7